Gene Details



FREM1 and homologs in 1 species are found in 107 GeneSets:


- Entrez   - GeneNetwork   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 2112 Genes GS210214: GO:0005576 extracellular region
Expand Tier I Human 63 Genes GS175327: HP:0000568 Microphthalmos
Expand Tier I Human GO 386 Genes GS207498: GO:0001501 skeletal system development
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human GO 11 Genes GS200240: GO:0097094 craniofacial suture morphogenesis
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 228 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human 32 Genes GS172787: HP:0001539 Omphalocele
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 43 Genes GS172862: HP:0000664 Synophrys
Expand Tier I Human 71 Genes GS174898: HP:0100887 Abnormality of globe size
Expand Tier I Human CTD 3168 Genes GS127127: Benzo(a)pyrene interacting genes (MeSH:D001564) in CTD
Expand Tier I Human 17 Genes GS172814: HP:0000336 Prominent supraorbital ridges
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human GO 361 Genes GS210217: GO:0005578 proteinaceous extracellular matrix
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human GO 186 Genes GS201254: GO:0044420 extracellular matrix part
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human GO 90 Genes GS208328: GO:0005604 basement membrane
Expand Tier I Human 840 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Human 10 Genes GS175118: HP:0000579 Nasolacrimal duct obstruction
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 178 Genes GS202566: GO:0048705 skeletal system morphogenesis
Expand Tier I Human GO 5764 Genes GS206742: GO:0043167 ion binding
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human GO 149 Genes GS198845: GO:0007160 cell-matrix adhesion
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 1587 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human 51 Genes GS172891: HP:0100538 Abnormality of the supraorbital ridges
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 167 Genes GS170916: HP:0008056 Aplasia/Hypoplasia affecting the eye
Expand Tier I Human 46 Genes GS173611: HP:0002219 Facial hypertrichosis
Expand Tier I Human 12 Genes GS175927: HP:0000243 Trigonocephaly
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 267 Genes GS196679: GO:0030246 carbohydrate binding
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human 27 Genes GS171447: HP:0000601 Hypotelorism
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 14 Genes GS171660: HP:0000614 Abnormality of the nasolacrimal system
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human GO 67 Genes GS195459: GO:0060349 bone morphogenesis
Expand Tier I Human GO 4003 Genes GS208978: GO:0043169 cation binding
Expand Tier I Human 18 Genes GS171885: HP:0000625 Cleft eyelid
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human GO 950 Genes GS195976: GO:0007155 cell adhesion
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 10 Genes GS172838: HP:0004122 Midline defect of the nose
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 44 Genes GS174484: HP:0000521 Abnormality of tear glands or tear production
Expand Tier I Human GO 792 Genes GS205616: GO:0009887 organ morphogenesis
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 521 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human GO 96 Genes GS195460: GO:0060348 bone development
Expand Tier I Human 48 Genes GS173103: HP:0004378 Abnormality of the anus
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Human GO 425 Genes GS196302: GO:0031012 extracellular matrix
Expand Tier I Human 8 Genes GS176456: HP:0001545 Anteriorly placed anus
Expand Tier I Human GO 216 Genes GS195701: GO:0031589 cell-substrate adhesion
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human 418 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human GO 952 Genes GS200151: GO:0022610 biological adhesion
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 12 Genes GS175372: HP:0011481 Abnormality of the lacrimal duct
Expand Tier I Human GO 1094 Genes GS201255: GO:0044421 extracellular region part
Expand Tier I Human 15 Genes GS175229: HP:0002025 Anal stenosis
Expand Tier I Human 195 Genes GS174236: HP:0000534 Abnormality of the eyebrow
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 182 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human GO 3902 Genes GS198323: GO:0046872 metal ion binding
Expand Tier I Human 61 Genes GS175740: HP:0010747 Medial flaring of the eyebrow
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human GO 4701 Genes GS195977: GO:0007154 cell communication
Expand Tier I Human 908 Genes GS175527: HP:0000006 Autosomal dominant inheritance
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 13 Genes GS173491: HP:0000528 Anophthalmia
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 19 Genes GS173649: HP:0004397 Ectopic anus
Expand Tier I Human GO 2539 Genes GS203335: GO:0048513 organ development
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen